Clinical effect of suction drainage on postoperative drainage after uniportal thoracoscopic lung cancer resection

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200064605

Enrollment

Unknown

Registered

2022-10-12

Start date

2022-10-12

Completion date

Unknown

Last updated

2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung nodules

Interventions

Suction group:None

Non-suction group:None

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Pathologically confirmed primary non-small cell lung cancer (NSCLC); 2. Uniporal lobectomy and segmentectomy with at least 3 lymph node stations dissected or sampled; 3. Drain tube is 20F silicone drain tube.

Exclusion criteria

Exclusion criteria: 1. Intraoperative bleeding is greater than 800ml; 2. Intraoperative conversion to open; 3. Patients receiving neoadjuvant treatment; 4. Applied suction due to persistent air leak or subcutaneous emphysema.

Design outcomes

Primary

Measure	Time frame
Chest tube duration;	—

Secondary

Measure	Time frame
Drainage volume;Pulmonary complication;Length of postoperative hospital stay;Hospitalization cost;	—

Countries

China

Contacts

Public ContactYang Qiu

West China Hospital of Sichuan University

5997394@qq.com+86 18382029913

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026